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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1071044생성일: 2026년 10월 27일

Dimethylformamide → 3-Tert-butyloxycarbonyl-6-(3-chloropropyl)-1,2,3,4,5,6-hexahydroazepino[4,5-b]indole

https://huagongshe.com/reaction/1071044

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참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물1-Bromo-3-chloropropaneHCID 8006—
반응물Sodium hydrideHCID 24758—
반응물tert-butyl 1,4,5,6-tetrahydroazepino[4,5-b]indole-3(2H)-carboxylateHCID 22396759—
용매Ethyl AcetateHCID 8857—
생성물3-Tert-butyloxycarbonyl-6-(3-chloropropyl)-1,2,3,4,5,6-hexahydroazepino[4,5-b]indoleHCID 22396630—

반응 조건

온도0 °C

반응 단계

Sodium hydride (335 mg, 60%) was added to a solution of 3-tert-butyloxycarbonyl 1,2,3,4,5,6-hexahydroazepino[4,5-b]indole (1.99 g) and DMF (21.0 mL) at 0° C. The solution was stirred at 0° C. for 30 min and then 1-bromo-3-chloropropane (0.74 mL) was added. The solution was stirred at 0° C. for 1 h and 16 h at room temperature. The solution was diluted with EtOAc, which was washed with water (3×20 mL). The combined aqueous layers were extracted with EtOAc (2×20 mL). The combined organic layers were dried (MgSO4), filtered, and concentrated. The crude material was purified by chromatography (Biotage, silica gel, 4:1-1:1 hexane:EtOAc) to give 1.38 g of the title compound as an oil: 1H NMR (300 MHz, CDCl3) δ 7.50, 7.10-7.40, 4.28, 3.55-3.82, 3.52, 2.95-3.10, 2.15-2.30, 1.51; MS (ESI) m/z 363 (M+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06903090B2
출처 데이터셋uspto-grants-2005_06
ORD IDord-308e0816e1a74a6ebfa8694cdf9ac572
출처 메모uspto-grants-2005_06